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Journal Abstract Search

301 related items for PubMed ID: 26485571

  • 1. Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.
    Muskett JA, Chattaraj P, Heneghan JF, Reimold FR, Shmukler BE, Brewer CC, King KA, Zalewski CK, Shawker TH, Butman JA, Kenna MA, Chien WW, Alper SL, Griffith AJ.
    Laryngoscope; 2016 Jul; 126(7):E240-7. PubMed ID: 26485571
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  • 2. Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss.
    Okamoto Y, Mutai H, Nakano A, Arimoto Y, Sugiuchi T, Masuda S, Morimoto N, Sakamoto H, Ogahara N, Takagi A, Taiji H, Kaga K, Ogawa K, Matsunaga T.
    Laryngoscope; 2014 Apr; 124(4):E134-40. PubMed ID: 24105851
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  • 4. Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.
    Song MH, Shin JW, Park HJ, Lee KA, Kim Y, Kim UK, Jeon JH, Choi JY.
    Laryngoscope; 2014 May; 124(5):E194-202. PubMed ID: 24338212
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  • 7. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct.
    Wang M, Zhang F, Xu L, Xiao Y, Li J, Fan Z, Sun Q, Bai X, Wang H.
    Int J Pediatr Otorhinolaryngol; 2016 Nov; 90():170-174. PubMed ID: 27729126
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  • 9. Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes.
    Choi BY, Madeo AC, King KA, Zalewski CK, Pryor SP, Muskett JA, Nance WE, Butman JA, Brewer CC, Griffith AJ.
    J Med Genet; 2009 Dec; 46(12):856-61. PubMed ID: 19578036
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  • 11. Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.
    Huang S, Han D, Yuan Y, Wang G, Kang D, Zhang X, Yan X, Meng X, Dong M, Dai P.
    J Transl Med; 2011 Sep 30; 9():167. PubMed ID: 21961810
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  • 13. Enlarged vestibular aqueduct: Audiological and genetical features in children and adolescents.
    Aimoni C, Ciorba A, Cerritelli L, Ceruti S, Skarżyński PH, Hatzopoulos S.
    Int J Pediatr Otorhinolaryngol; 2017 Oct 30; 101():254-258. PubMed ID: 28780189
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  • 14. Pathogenic substitution of IVS15 + 5G > A in SLC26A4 in patients of Okinawa Islands with enlarged vestibular aqueduct syndrome or Pendred syndrome.
    Ganaha A, Kaname T, Yanagi K, Naritomi K, Tono T, Usami S, Suzuki M.
    BMC Med Genet; 2013 May 24; 14():56. PubMed ID: 23705809
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  • 17. Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct.
    Chattaraj P, Reimold FR, Muskett JA, Shmukler BE, Chien WW, Madeo AC, Pryor SP, Zalewski CK, Butman JA, Brewer CC, Kenna MA, Alper SL, Griffith AJ.
    JAMA Otolaryngol Head Neck Surg; 2013 Sep 24; 139(9):907-13. PubMed ID: 24051746
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  • 18. [Correlation of temporal bone HRCT, SLC26A4 gene and hearing loss in enlarged vestibular aqueduct].
    Zhao Z, Zhu Y, Fu Y, Jiang H.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2022 Oct 24; 36(10):736-740. PubMed ID: 36217650
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